Multi-polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Yingjie Shi, Emma Sprooten, Peter Mulders, Janna Vrijsen, Janita Bralten, Ditte Demontis, Anders D. Børglum, G. Bragi Walters, Kari Stefansson, Philip van Eijndhoven, Indira Tendolkar, Barbara Franke, Nina Roth Mota
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Abstract

The dense co-occurrence of psychiatric disorders questions the categorical classification tradition and motivates efforts to establish dimensional constructs with neurobiological foundations that transcend diagnostic boundaries. In this study, we examined the genetic liability for eight major psychiatric disorder phenotypes under both a disorder-specific and a transdiagnostic framework. The study sample (n = 513) was deeply phenotyped, consisting of 452 patients from tertiary care with mood disorders, anxiety disorders (ANX), attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorders, and/or substance use disorders (SUD) and 61 unaffected comparison individuals. We computed subject-specific polygenic risk score (PRS) profiles and assessed their associations with psychiatric diagnoses, comorbidity status, as well as cross-disorder behavioral dimensions derived from a rich battery of psychopathology assessments. High PRSs for depression were unselectively associated with the diagnosis of SUD, ADHD, ANX, and mood disorders (p < 1e-4). In the dimensional approach, four distinct functional domains were uncovered, namely the negative valence, social, cognitive, and regulatory systems, closely matching the major functional domains proposed by the Research Domain Criteria (RDoC) framework. Critically, the genetic predisposition for depression was selectively reflected in the functional aspect of negative valence systems (R2 = 0.041, p = 5e-4) but not others. This study adds evidence to the ongoing discussion about the misalignment between current psychiatric nosology and the underlying psychiatric genetic etiology and underscores the effectiveness of the dimensional approach in both the functional characterization of psychiatric patients and the delineation of the genetic liability for psychiatric disorders.

Abstract Image

精神病学中的多基因评分:从疾病特异性到跨诊断视角。
精神疾病的密集并发对分类传统提出了质疑,并促使人们努力建立具有超越诊断界限的神经生物学基础的维度结构。在这项研究中,我们在疾病特异性和跨诊断框架下检查了八种主要精神疾病表型的遗传责任。研究样本(n = 513)是深度表型,包括452名来自三级护理的情绪障碍、焦虑障碍(ANX)、注意力缺陷/多动障碍(ADHD)、自闭症谱系障碍和/或物质使用障碍(SUD)患者和61名未受影响的对照个体。我们计算了受试者特异性多基因风险评分(PRS)档案,并评估了它们与精神病诊断、共病状态以及从丰富的精神病理学评估中得出的跨障碍行为维度的关系。抑郁症的高PRS与SUD、ADHD、ANX和情绪障碍的诊断无关(p 2. = 0.041,p = 5e-4),而不是其它。这项研究为正在进行的关于当前精神疾病学和潜在精神遗传病因之间不一致的讨论提供了证据,并强调了维度方法在精神病患者功能表征和精神疾病遗传责任描述方面的有效性。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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